Standout Papers
- Genome-wide changes in lncRNA, splicing, and regional gene expression patterns in autism (2016)
- A framework for variation discovery and genotyping using next-generation DNA sequencing data (2011)
- From FastQ Data to High‐Confidence Variant Calls: The Genome Analysis Toolkit Best Practices Pipeline (2013)
- Inherited and De Novo Genetic Risk for Autism Impacts Shared Networks (2019)
Immediate Impact
12 by Nobel laureates 35 from Science/Nature 59 standout
Citing Papers
Accurate proteome-wide missense variant effect prediction with AlphaMissense
2023 StandoutScienceNobel
Y chromosome loss in cancer drives growth by evasion of adaptive immunity
2023 StandoutNature
Works of Christopher Hartl being referenced
A framework for variation discovery and genotyping using next-generation DNA sequencing data
2011 Standout
Author Peers
| Author | Last Decade | Papers | Cites | ||||
|---|---|---|---|---|---|---|---|
| Christopher Hartl | 6453 | 5345 | 451 | 1956 | 14 | 12.4k | |
| Guillermo del Angel | 5712 | 4843 | 96 | 1832 | 13 | 11.4k | |
| Ryan Poplin | 6517 | 5156 | 125 | 1993 | 11 | 13.6k | |
| Jared Maguire | 4369 | 3675 | 67 | 1451 | 8 | 8.3k | |
| Ben Fry | 8758 | 7001 | 553 | 1566 | 27 | 19.4k | |
| Anushya Muruganujan | 7851 | 2065 | 111 | 1541 | 16 | 12.5k | |
| Anthony Philippakis | 6414 | 3904 | 95 | 1482 | 67 | 11.2k | |
| Manuel A. Rivas | 4215 | 3507 | 75 | 1328 | 5 | 8.2k | |
| Pauline C. Ng | 7172 | 5059 | 128 | 1377 | 23 | 12.2k | |
| Pablo Cingolani | 3663 | 2968 | 48 | 979 | 17 | 8.2k | |
| D.B. Bender | 6562 | 12535 | 3027 | 1666 | 33 | 23.9k |
All Works
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